The steroid pregnenolone sulfate (PREGS) may be one of the factors responsible for the memory decline related to normal aging or associated with Alzheimer's disease (AD). The purpose of this study is to determine whether plasma levels of PREGS are decreased patients with at mild to moderate AD compared with AD-free control subjects matched for gender and age and to see whether they are inversely correlated with the severity of memory deficits in AD patients. The hypothesis is that blood levels of PREGS are decreased with advanced age and with the stage of AD that would be positively correlated with memory deficits. Therefore PREGS could be considered as an early marker of the memory deficits in AD.
PREGS is a derivative of pregnenolone which the obligatory precursor of all steroid hormones originating from the gonads and adrenal glands. In rodents, PREGS has been demonstrated to improve memory performance in various behavioural tests. In humans, PREGS is one the most abundant circulating steroids. There are some indications about its decrease in blood during aging, and in brain samples from aged patients with AD, low concentrations of PREGS have been correlated with high levels of beta-amyloid peptide and phosphorylated tau protein. To date, a precise and rigorous evaluation of PREGS blood concentrations during aging is lacking and the relationship between these concentrations and the memory loss associated with AD has not been established. Primary objective To show that plasma concentrations of PREGS are decreased in AD patients (" case ") compared to free-AD subjects (" controls "), matched for gender and age. Secondary objectives * To show that plasma concentrations of PREGS are inversely correlated with the severity of memory deficits in AD patients. * To show that plasma concentrations of PREGS are correlated with the memory scores in the controls. * To show that plasma concentrations of PREGS decrease in the controls. * To search for a relationship between some of PREGS metabolites and age or the severity of memory deficits. This is a case-control study that will comprise 200 subjects aged over 70 years, including 100 outpatients with mild to moderate AD and 100 AD-free volunteer controls matched on age and gender. These two groups will be stratified into age-sub-groups \[70-74\] \[75-79\] \[80-84\] \[85-89\] \> 90 years and will include 10 men and 10 women per sub-group. AD patients and controls will be enrolled and evaluated in the geriatric centres of 5 hospitals namely BICETRE, BROCA, PAUL BROUSSE, PITIE-SALPETRIERE and ROTHSCHILD. They will all be submitted to a clinical examination, biological analyses, cognitive tests and a brain magnetic resonance imaging scan. Blood will be collected from all subjects for steroid analysis by gas chromatography-mass spectrometry, a sensitive and accurate methodology that allows simultaneous quantification of several steroids in the same individual sample. PREGS and some of its metabolites will be identified and quantified at the "Institute medical of heath" (INSERM U788).
Study Type
OBSERVATIONAL
Enrollment
90
Assistance publique - Hôpitaux de Paris Hôpital Bicêtre
Le Kremlin-Bicêtre, France
Inserm Umr 788
Le Kremlin-Bicêtre, France
AP-HP Hôpital Rothschild
Paris, France
Assistance Publique - Hôpitaux de Paris Hôpital Broca
Paris, France
Assistance Publique - Hôpitaux de Paris, Hôpital Pitié-Salpétrière
Paris, France
Assistance Publique - Hôpitaux de Paris, Hôpital Paul Brousse
Villejuif, France
Plasma concentrations of PREGS determined by GC-MS
Time frame: At the day of diagnostic blood collection
Memory scores of the RL-RI test according to the GROBER and BUSCKE test
Time frame: At the day of blood collection
Plasma concentrations of PREGS metabolites
Time frame: At the day of blood collection
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